Cargando…

Genetic variations associated with telomere length affect the risk of gastric carcinoma

This study aimed to further understand the role of relative telomere length (RTL) in susceptibility to gastric carcinoma (GC) and investigate the association between genetic polymorphisms in the telomere length related genes and GC risk. RTL was measured using the real-time quantitative polymerase c...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lili, Ma, Yuxiang, Fan, Zhongcheng, Han, Ying, Su, Ru, Chen, Rong, Xu, Jiang, Liu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2020
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306382/ https://www.ncbi.nlm.nih.gov/pubmed/32502020 http://dx.doi.org/10.1097/MD.0000000000020551

Ejemplares similares

Clinicopathological characteristics of TERT promoter mutation and telomere length in hepatocellular carcinoma
por: Lee, Hye Won, et al.
Publicado: (2017)

Association between genetic polymorphism of telomere-associated gene ACYP2 and the risk of HAPE among the Chinese Han population: A Case–control study
por: Zhu, Linhao, et al.
Publicado: (2017)

Genetic Variations in Key MicroRNAs are Associated With the Survival of Nonsmall Cell Lung Cancer
por: Wu, Shuangshuang, et al.
Publicado: (2015)

Association between regulator of telomere elongation helicase1 (RTEL1) gene and HAPE risk: A case-control study
por: Rong, Hao, et al.
Publicado: (2017)

Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
por: Dai, Zhi-Jun, et al.
Publicado: (2016)

Platelet count and gastric cancer susceptibility: A Mendelian randomization study
por: Zhu, Yingze, et al.
Publicado: (2023)

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report
por: Zhang, HaoZheng, et al.
Publicado: (2023)

Chromosomal copy number variations in products of conception from spontaneous abortion by next-generation sequencing technology
por: Dai, Rulin, et al.
Publicado: (2019)

Association Between Genetic Polymorphisms in the Promoter Regions of Let-7 and Risk of Papillary Thyroid Carcinoma: A Case-Control Study
por: Wang, Yichao, et al.
Publicado: (2015)

Association between PRKAA1 rs13361707 T>C polymorphism and gastric cancer risk: Evidence based on a meta-analysis
por: Jiang, You, et al.
Publicado: (2018)

Papillary thyroid carcinoma with hyperthyroidism and multiple metastases: A case report
por: Zhang, Li-li, et al.
Publicado: (2020)

Phenotypic spectrum and genetic analysis in the fatal cases of Schaaf-Yang syndrome: Two case reports and literature review
por: Chen, Xuefei, et al.
Publicado: (2020)

Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
por: Hu, Hua, et al.
Publicado: (2021)

Nuclear Factor-Kappa B1 is Associated With Gastric Cancer in a Chinese Population
por: Hua, Tang, et al.
Publicado: (2014)

The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study
por: Lyu, Mengyuan, et al.
Publicado: (2019)

Common genetic variants in the FETUB locus, genetically predicted fetuin-B levels, and risk of insulin resistance in obese Chinese adults
por: Li, Zhibin, et al.
Publicado: (2017)

De Novo mutation of FOXF1 causes alveolar capillary dysplasia with misalignment of pulmonary veins: A case report
por: Deng, Lili, et al.
Publicado: (2021)

Clinical and Genetic Factors Associated With Thiazide-Induced Hyponatremia
por: Huang, Chin-Chou, et al.
Publicado: (2015)

Association of lncRNA SOX2OT rs9839776 polymorphism with gastric cancer risk in Korean: Case-control study
por: Hong, Jang Hee, et al.
Publicado: (2023)

Thyroid hormone resistance and the value of genetics: Three case reports
por: Xiao, Xiao, et al.
Publicado: (2019)

Proceedings of the 23(rd) Annual Meeting of the Portuguese Society of Human Genetics
Publicado: (2020)

Clinical and genetic features of four patients with Pearson syndrome: An observational study
por: Son, Ji Soo, et al.
Publicado: (2022)

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor
por: Ayuso, Pedro, et al.
Publicado: (2015)

Association of Genetic Polymorphisms on VEGFA and VEGFR2 With Risk of Coronary Heart Disease
por: Liu, Doxing, et al.
Publicado: (2016)

Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report
por: Wang, Zhankui, et al.
Publicado: (2021)

An elective radiation dose of 46 Gy is feasible in nasopharyngeal carcinoma treated by intensity-modulated radiotherapy: A long-term follow-up result
por: Hung, Tsung-Min, et al.
Publicado: (2017)

Interaction between ALDH2 rs671 and life habits affects the risk of hypertension in Koreans: A STROBE observational study
por: Kim, Sung-Soo, et al.
Publicado: (2021)

Genetic analysis and management of a familial hypercholesterolemia pedigree with polygenic variants: Case report
por: Han, Yu, et al.
Publicado: (2023)

Multiple adverse drug reactions and genetic polymorphism testing: A case report with negative result
por: Arellano, Ana Lucía, et al.
Publicado: (2017)

Pharmacogenetic and case–control study on potassium channel related gene variants and genetic generalized epilepsy
por: Qu, Jian, et al.
Publicado: (2017)

Role of surfactant protein C in neonatal genetic disorders of the surfactant system: A case report
por: Tan, Ya-Xin, et al.
Publicado: (2021)

The association of CDKN2BAS gene polymorphisms and intracranial aneurysm: A meta-analysis
por: Yu, Ting, et al.
Publicado: (2020)

Gene polymorphisms (rs324957, rs324981) in NPSR1 are associated with increased risk of primary insomnia: A cross-sectional study
por: Xie, Yuping, et al.
Publicado: (2020)

Prenatal detection of pure proximal 6q14.1 microduplication encompassing LCA5 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2022)

Determinants of Plasma Renin Activity: Role of a Human Renin Gene Variant as a Genetic Factor
por: Konoshita, Tadashi, et al.
Publicado: (2014)

Prenatal diagnosis and genetic analysis of a fetus with Branchio-oto-renal syndrome: A case report
por: Tang, Ping, et al.
Publicado: (2022)

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study
por: Cai, Meiying, et al.
Publicado: (2022)

Preimplantation genetic testing and prenatal diagnosis in a family with pseudovaginal perineoscrotal hypospadias: A case report
por: Chen, Jiayao, et al.
Publicado: (2023)

Correlation between SHBG gene polymorphism and male infertility in Han population of Henan province of China: A STROBE-compliant article
por: Cui, Yuan-rong, et al.
Publicado: (2017)

Clinical and genetic factors associated with warfarin maintenance dose in northern Chinese patients with mechanical heart valve replacement
por: Liu, Rui, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_k2pu1n36garjqdosqb0p0f6njn